Skip to main navigation menu Skip to main content Skip to site footer

Review Articles

Vol. 13 No. sp2 (2026): Recent Advances in Agriculture

Enhancing crop resilience and productivity through optimised nutrient management under abiotic and biotic stresses

DOI
https://doi.org/10.14719/pst.12653
Submitted
9 November 2025
Published
05-06-2026

Abstract

Plants continuously encounter a wide range of biotic and abiotic stresses that adversely influence physiological, biochemical and metabolic processes, leading to substantial yield losses worldwide. Abiotic stresses such as drought, salinity, heat, waterlogging and heavy metal toxicity disrupt cellular homeostasis and photosynthetic efficiency, while biotic agents, including pathogens, pests, nematodes and weeds further compromise plant growth and productivity. Nutrient management plays a pivotal role in enhancing plant resilience to these stressors. Balanced application of macronutrients (sodium (N), phosphorus (P), potassium (K), calcium (Ca), magnesium (Mg), sulfur (S)), micronutrients like zinc (Zn), iron (Fe), boron (B), copper (Cu)) and beneficial elements such as silicon not only sustains physiological functioning but also activates antioxidant defence systems, osmotic regulation and cellular detoxification mechanisms. Nutrient management, combining chemical fertilisers with organic amendments and microbial inoculants, strengthens root development, improves water and nutrient use efficiency and enhances stress tolerance through synergistic nutrient interactions. This review provides a comprehensive synthesis of current knowledge on the physiological roles of essential nutrients in mitigating plant stresses, evaluates their mechanisms of action and highlights sustainable management strategies that harmonise productivity with environmental stewardship. This review synthesises the integrative role of plant nutrients in reinforcing physiological and biochemical defence mechanisms and highlights future research priorities essential for developing climate-resilient crop production strategies.

 

References

  1. 1. Bashir K, Matsui A, Rasheed S, Seki M. Recent advances in the characterisation of plant transcriptomes in response to drought, salinity, heat and cold stress. F1000Res. 2019;8:658. https://doi.org/10.12688/f1000research.18424.1
  2. 2. Dong Q, Wallrad L, Almutairi BO, Kudla J. Ca2+ signalling in plant responses to abiotic stresses. J Integr Plant Biol. 2022;64:287–300. https://doi.org/10.1111/jipb.13228
  3. 3. Fahad S, Bajwa AA, Nazir U, Anjum SA, Farooq A, Zohaib A, et al. Crop production under drought and heat stress: plant responses and management options. Front Plant Sci. 2017;8:1147. https://doi.org/10.3389/fpls.2017.01147
  4. 4. Ahmad P, Sarwat M, Bhat NA, Wani MR, Kazi AG, Tran LP. Alleviation of cadmium toxicity in Brassica juncea L. (Czern. & Coss.) by calcium application involves various physiological and biochemical strategies. PLoS One. 2015;10:e0114571. https://doi.org/10.1371/journal.pone.0114571
  5. 5. Salehi-Lisar SY, Bakhshayeshan-Agdam H. Drought stress in plants: causes, consequences and tolerance. In: Hossain MA, Wani SH, Bhattacharjee S, Burritt DJ, Tran LS, editors. Drought stress tolerance in plants. Vol. 1. Cham (Switzerland): Springer International Publishing; 2016. p. 1–16. https://doi.org/10.1007/978-3-319-28899-4_1
  6. 6. Zhang GX, Gan TY, Su XL. Twenty-first century drought analysis across China under climate change. Clim Dyn. 2022;59:1665–85. https://doi.org/10.1007/s00382-021-06064-5
  7. 7. Saini DK, Impa SM, McCallister D, Patil GB, Abidi N, Ritchie G, et al. High day and night temperatures impact on cotton yield and quality: current status and future research direction. J Cotton Res. 2023;6:16. https://doi.org/10.1186/s42397-023-00154-x
  8. 8. Pei YY, Lei L, Fan XW, Li YZ. Effects of high air temperature, drought and both combinations on maize: a case study. Plant Sci. 2023;327:111543. https://doi.org/10.1016/j.plantsci.2022.111543
  9. 9. Ghosh PK, Jeer M, Sivalingam PN, Parmeshwari B, Singh HK, Choudhary VK, et al. Agronomic innovations in biotic stress management and its combined effect with abiotic stresses in crop production. Indian J Agron. 2021;66(Special Issue 5th IAC):S237–57.
  10. 10. Zulfiqar F, Younis A, Riaz A, Mansoor F, Hameed M, Akram NA, et al. Morpho-anatomical adaptations of two Tagetes erecta L. cultivars with contrasting response to drought stress. Pak J Bot. 2020;52:801–10. https://doi.org/10.30848/PJB2020-3(35)
  11. 11. Deepak SB, Thakur A, Singh S, Bakshi M, Bansal S. Changes in crop physiology under drought stress: a review. J Pharmacogn Phytochem. 2019;8:1251–3.
  12. 12. Bheemanahalli R, Ramamoorthy P, Poudel S, Samiappan S, Wijewardane N, Reddy KR. Effects of drought and heat stresses during reproductive stage on pollen germination, yield and leaf reflectance properties in maize (Zea mays L.). Plant Direct. 2022;6(8):e434. https://doi.org/10.1002/pld3.434
  13. 13. Hu W, Huang Y, Bai H, Liu Y, Wang S, Zhou Z. Influence of drought stress on pistil physiology and reproductive success of two Gossypium hirsutum cultivars differing in drought tolerance. Physiol Plant. 2020;168:909–20. https://doi.org/10.1111/ppl.13030
  14. 14. Zhang J, Loka DA, Wang J, Ran Y, Shao C, Tuersun G, et al. Co-occurring elevated temperature and drought stress inhibit cotton pollen fertility by disturbing anther carbohydrate and energy metabolism. Ind Crops Prod. 2024;208:115348. https://doi.org/10.1016/j.indcrop.2022.115348
  15. 15. Poudel S, Vennam RR, Sankarapillai LV, Liu J, Reddy KR, Wijewardane NK, et al. Negative synergistic effects of drought and heat during flowering and seed setting in soybean. Environ Exp Bot. 2024;222:105769. https://doi.org/10.1016/j.envexpbot.2024.105769
  16. 16. Shrivasata P, Kumar R. Soil salinity: a serious environmental issue and plant growth-promoting bacteria as one of the tools for its alleviation. Saudi J Biol Sci. 2015;22:123–31. https://doi.org/10.1016/j.sjbs.2014.12.001
  17. 17. Nachshon U. Cropland soil salinisation and associated hydrology: trends, processes and examples. Water. 2018;10(8):1030. https://doi.org/10.3390/w10081030
  18. 18. Negacz K, Malek Ž, de Vos A, Vellinga P. Saline soils worldwide: identifying the most promising areas for saline agriculture. J Arid Environ. 2022;203:104775. https://doi.org/10.1016/j.jaridenv.2022.104775
  19. 19. Nadeem M, Tariq MN, Amjad M, Sajjad M, Akram M, Imran M, et al. Salinity induced changes in the nutritional quality of bread wheat (Triticum aestivum L.) genotypes. Agrivita. 2020;42:1–12. https://doi.org/10.17503/agrivita.v42i1.2273
  20. 20. El Sabagh A, Islam MS, Skalicky M, Ali Raza M, Singh K, Hossain M, et al. Salinity stress in wheat (Triticum aestivum L.) in the changing climate: adaptation and management strategies. Front Agron. 2021;3:661932. https://doi.org/10.3389/fagro.2021.661932
  21. 21. Parvin K, Haque MN. Protective role of salicylic acid on salt-affected broccoli plant. J Agric Ecol Res. 2017;10(2). https://doi.org/10.9734/JAERI/2017/30142
  22. 22. Hoang TML, Moghaddam L, Williams B, Khanna H, Dale J, Mundree SG. Development of salinity tolerance in rice by constitutive overexpression of genes involved in the regulation of programmed cell death. Front Plant Sci. 2015;6:175. https://doi.org/10.3389/fpls.2015.00175
  23. 23. Yadav T, Kumar A, Yadav RK, Yadav G, Kumar R, Kushwaha M. Salicylic acid and thiourea mitigate the salinity and drought stress on physiological traits governing yield in pearl millet–wheat. Saudi J Biol Sci. 2020;27(8):2010–7. https://doi.org/10.1016/j.sjbs.2020.06.030
  24. 24. Zorb C, Geilfus CM, Dietz KJ. Salinity and crop yield. Plant Biol. 2018;21:31–8. https://doi.org/10.1111/plb.12884
  25. 25. Atieno J, Li Y, Langridge P, Dowling K, Brien C, Berger B, et al. Exploring genetic variation for salinity tolerance in chickpea using image-based phenotyping. Sci Rep. 2017;7(1):1–11. https://doi.org/10.1038/s41598-017-01211-7
  26. 26. Ikuyinminu E, Goñi O, O’Connell S. Enhancing irrigation salinity stress tolerance and increasing yield in tomato using a precision-engineered protein hydrolysate and Ascophyllum nodosum-derived biostimulant. Agron. 2022;12(4):809. https://doi.org/10.3390/agronomy12040809
  27. 27. Sanwal SK, Kumar P, Kesh H, Gupta VK, Kumar A, Kumar A, et al. Salinity stress tolerance in potato cultivars: evidence from physiological and biochemical traits. Plants (Basel). 2022;11(14):1842. https://doi.org/10.3390/plants11141842
  28. 28. Kurunc A. Effects of water and salinity stresses on growth, yield and water use of iceberg lettuce. J Sci Food Agric. 2021;101(13):5688–96. https://doi.org/10.1002/jsfa.11223
  29. 29. Costa DW. A review of the possible impacts of climate change on forests in the humid tropics. J Natl Sci Found Sri Lanka. 2011;39:281–302. https://doi.org/10.4038/jnsfsr.v39i4.3879
  30. 30. Chen Q, Cao X, Nie X, Li Y, Liang T, Ci L. Alleviation role of functional carbon nanodots for tomato growth and soil environment under drought stress. J Hazard Mater. 2022;423:127260. https://doi.org/10.1016/j.jhazmat.2021.127260
  31. 31. Chen QH, Yang GW. Signal function studies of ROS, especially RBOH-dependent ROS, in plant growth, development and environmental stress. J Plant Growth Regul. 2020;39:157–71. https://doi.org/10.1007/s00344-019-09971-4
  32. 32. Xu Y, Wu Y, Han Y, Song J, Zhang W, Han W, et al. Effect of chemical regulators on the recovery of leaf physiology, dry matter accumulation and translocation and yield-related characteristics in winter wheat following dry-hot wind. J Integr Agric. 2024;23:108–21. https://doi.org/10.1016/j.jia.2023.04.019
  33. 33. Zhao C, Liu B, Piao S, Wang X, Lobell DB, Huang Y, et al. Temperature increase reduces global yields of major crops in four independent estimates. Proc Natl Acad Sci U S A. 2017;114:9326–31. https://doi.org/10.1073/pnas.1701762114
  34. 34. Hatfield JL, Boote KJ, Kimball BA, Ziska LH, Izaurralde RC, Ort D. Climate impacts on agriculture: implications for crop production. Agron J. 2011;103:351–70. https://doi.org/10.2134/agronj2010.0303
  35. 35. Zahra N, Hafeez MB, Ghaffar A, Kausar A, Zeidi MA, Siddique KHM, et al. Plant photosynthesis under heat stress: effects and management. Environ Exp Bot. 2023;206:105178. https://doi.org/10.1016/j.envexpbot.2022.105178
  36. 36. Bassu S, Brisson N, Durand JL, Boote K, Lizaso J, Jones JW, et al. How do various maize crop models vary in their responses to climate change factors? Glob Chang Biol. 2014;20(7):2301–20. https://doi.org/10.1111/gcb.12520
  37. 37. Balla K, Rakszegi M, Li Z, Békés F, Bencze S, Veisz O. Quality of winter wheat in relation to heat and drought shock after anthesis. Czech J Food Sci. 2011;29:117–28. https://doi.org/10.17221/227/2010-CJFS
  38. 38. Cao YY, Duan H, Yang LN, Wang ZQ, Liu LJ, Yang JC. Effect of high temperature during heading and early filling on grain yield and physiological characteristics in indica rice. Acta Agron Sin. 2009;35:512–21. https://doi.org/10.1016/S1875-2780(08)60071-1
  39. 39. Tack J, Lingenfelser J, Jagadish SVK. Disaggregating sorghum yield reductions under warming scenarios exposes narrow genetic diversity in US breeding programs. Proc Natl Acad Sci U S A. 2017;114:9296–301. https://doi.org/10.1073/pnas.1706383114
  40. 40. Schlenker W, Roberts MJ. Nonlinear temperature effects indicate severe damages to U.S. crop yields under climate change. Proc Natl Acad Sci U S A. 2009;106:15594–8. https://doi.org/10.1073/pnas.0906865106
  41. 41. Debaeke P, Casadebaig P, Flenet F, Langlade N. Sunflower crop and climate change: vulnerability, adaptation and mitigation potential from case studies in Europe. OCL. 2017;24(1):D102. https://doi.org/10.1051/ocl/2016052
  42. 42. Ayenan MAT, Danquah A, Hanson P, Asante IK, Danquah EY. Tomato (Solanum lycopersicum L.) genotypes respond differently to long-term dry and humid heat stress. Horticulturae. 2022;8(2):118. https://doi.org/10.3390/horticulturae8020118
  43. 43. Park B, Kim S, Kim S. Simulation of the impacts of high temperature stress on pepper (Capsicum annuum L.) yields. Front Plant Sci. 2025;16. https://doi.org/10.3389/fpls.2025.1590193
  44. 44. Yan K, Zhao S, Cui M, Han G, Wen P. Vulnerability of photosynthesis and photosystem I in Jerusalem artichoke (Helianthus tuberosus L.) exposed to waterlogging. Plant Physiol Biochem. 2018;125:239–46. https://doi.org/10.1016/j.plaphy.2018.02.017
  45. 45. Pais IP, Moreira R, Semedo JN, Ramalho JC, Lidon FC, Coutinho J, et al. Wheat crop under waterlogging: potential soil and plant effects. Plants (Basel). 2022;12:1987. https://doi.org/10.3390/plants12010149
  46. 46. Marashi SK. Evaluation of uptake rate and distribution of nutrient ions in wheat (Triticum aestivum L.) under waterlogging conditions. Iran J Plant Physiol. 2018;8:2539–47. https://doi.org/10.22034/ijpp.2018.543416
  47. 47. Huang C, Yang G, An ZQ, Zu GL, Ben A, Dong FN, et al. Effects of waterlogging at different stages and durations on maize growth and grain yields. Agric Water Manag. 2022;261:107334. https://doi.org/10.1016/j.agwat.2021.107334
  48. 48. Zhang Y, Chen Y, Lu H, Kong X, Dai J, Li Z, et al. Growth, lint yield and changes in physiological attributes of cotton under temporal waterlogging. Field Crops Res. 2016;194:83–93. https://doi.org/10.1016/j.fcr.2016.05.006
  49. 49. Mahoney KJ, Klapwyk JH, Stewart GA, Jay WS, Hooker DC. Agronomic management strategies to reduce the yield loss associated with spring harvested corn in Ontario. Am J Plant Sci. 2015;6:372. https://doi.org/10.4236/ajps.2015.62043
  50. 50. Li C, Chang Y, Luo Y, Li W, Jin M, Wang Y, et al. Nitrogen regulates stem lodging resistance by breaking the balance of photosynthetic carbon allocation in wheat. Field Crops Res. 2023;296:108908. https://doi.org/10.1016/j.fcr.2023.108908
  51. 51. Xue J, Gao S, Fan Y, Li L, Ming B, Wang K, et al. Traits of plant morphology, stalk mechanical strength and biomass accumulation in the selection of lodging-resistant maize cultivars. Eur J Agron. 2020;117:126073. https://doi.org/10.1016/j.eja.2020.126073
  52. 52. Zheng Z, Guo B, Dutta S, Roy V, Liu H, Schnable PS. The 2020 derecho revealed limited overlap between maize genes associated with root lodging and root system architecture. Plant Physiol. 2023;192:2394–403. https://doi.org/10.1093/plphys/kiad194
  53. 53. Farlex I. Definition: environment. The Free Dictionary. USA: Farlex Inc. Publishing; 2005.
  54. 54. Wintz H, Fox T, Vulpe C. Responses of plants to iron, zinc and copper deficiencies. Biochem Soc Trans. 2002;30:766–8. https://doi.org/10.1042/BST0300766
  55. 55. Rizvi A, Almas Zaidi F, Ameen F, Ahmed B, AlKahtani MDF, Khan MS. Heavy metal-induced stress on wheat: phytotoxicity and microbiological management. RSC Adv. 2020;10:38379–403. https://doi.org/10.1039/D0RA05610C
  56. 56. Rashid A, Schutte BJ, Ulery A, Deyholos MK, Sanogo S, Lehnhoff EA, et al. Heavy metal contamination in agricultural soil: environmental pollutants affecting crop health. Agron. 2023;13(6):1521. https://doi.org/10.3390/agronomy13061521
  57. 57. Din AMU, Mao HT, Khan A, Raza MA, Ahmed M, Yuan M, et al. Photosystems and antioxidative system of rye, wheat and triticale under Pb stress. Ecotoxicol Environ Saf. 2023;249:114356. https://doi.org/10.1016/j.ecoenv.2022.114356
  58. 58. Saleh SR, Kandeel MM, Ghareeb D, Ghoneim TM, Talha NI, Alaoui-Sosse B, et al. Wheat biological responses to stress caused by cadmium, nickel and lead. Sci Total Environ. 2020;706:136013. https://doi.org/10.1016/j.scitotenv.2019.136013
  59. 59. Rathee M, Dalal P. Emerging insect pests in Indian agriculture. Indian J Entomol. 2018;80:267–81. https://doi.org/10.5958/0974-8172.2018.00043.3
  60. 60. Dhawan AK, Singh K, Saini S, Mohindru B, Kaur A, Singh G, et al. Incidence and damage potential of mealybug, Phenacoccus solenopsis Tinsley on cotton in Punjab. Indian J Ecol. 2007;34:110–6.
  61. 61. Kranthi KR. Let not the whitefly see red. In: Singh A, editor. Cotton Statistics and News. Mumbai: Cotton Association of India; 2016. p. 1–6.
  62. 62. Nagaraja A, Chethana BS, Jain AK. Biotic stresses and their management. In: Millets and Pseudo Cereals. Elsevier; 2021. p. 119–42. https://doi.org/10.1016/B978-0-12-820089-6.00007-0
  63. 63. Ngele KK, Kalu UN. Studies on different species of plant parasitic nematodes attacking vegetable crops grown in Afikpo North L.G.A., Nigeria. Direct Res J Agric Food Sci. 2015;3(4):88–92.
  64. 64. Nicol JM, Turner SJ, Coyne D, De Nijs L, Hockland S, Maafi ZT. Genomics and molecular genetics of plant–nematode interactions. In: Current Nematode Threats to World Agriculture. Dordrecht: Springer; 2011. p. 21–43. https://doi.org/10.1007/978-94-007-0434-3_2
  65. 65. Kumari VV, Nath R, Sengupta K, Banerjee S, Dutta D, Karmakar S. Effect of date of sowing and foliar spray of micronutrients on growth, phenology, yield and seed quality of lentil (Lens culinaris) in New Alluvial Zone of West Bengal. Indian J Agric Sci. 2021;91:573–6. https://doi.org/10.56093/ijas.v91i4.112678
  66. 66. Anwar MP, Islam AKMM, Yeasmin S, Rashid MH, Juraimi AS, Ahmed S, et al. Weeds and their responses to management efforts in a changing climate. Agron. 2021;11(10):1921. https://doi.org/10.3390/agronomy11101921
  67. 67. Dixit A, Gogoi AK, Varshney JG. Weed atlas: district-wise distribution pattern of major weed flora in prominent crops. Jabalpur: National Research Centre for Weed Science; 2008.
  68. 68. Subudhi HN, Panda SP, Behera PK, Patnaik C. A checklist of weeds in rice fields of coastal Orissa. J Agric Sci. 2015;7:207–16. https://doi.org/10.5539/jas.v7n6p207
  69. 69. Punia SS, Yadav D, Amarjeet, Sindhu V. Investigation on weed flora of wheat in Haryana. Agric Res J. 2017;54:136–8. https://doi.org/10.5958/2395-146X.2017.00027.8
  70. 70. Nalini K, Murhukrishnan P, Chinnusamy C, Vennila C. Weeds of cotton: a review. Agric Rev. 2015;36:140–6. https://doi.org/10.5958/0976-0741.2015.00016.1
  71. 71. Jeyaraman S, Karamathullah J, Kannappan K, Padmanabhan D. Weed management studies in sugarcane: a review. Cooperative Sugar. 2002;34:207–17.
  72. 72. Choudhury PP, Singh R. Role of herbicides in agriculture. Indian Farming. 2015;65:66–72.
  73. 73. Singh R, Das TK, Kaur R, Raj R, Shekhawat K. Weed management in dryland agriculture in India for enhanced resource use efficiency and livelihood security. Proc Natl Acad Sci India B. 2016. https://doi.org/10.1007/s40011-016-0795-y
  74. 74. Yaduraju NT, Prasad Babu MBB, Poonam C. Herbicide use. In: Swaminathan MS, Chadha KL, editors. Agriculture and Environment. New Delhi: Malhotra Publishing House; 2006. p. 192–210.
  75. 75. Das SK, Avasthe RK. Plant nutrition management strategy: a policy for optimum yield. Acta Sci Agric. 2018;2(5):65–70.
  76. 76. Srinivasarao C, Subha Lakshmi C, Kundu S, Ranjith Kumar G, Manasa R, Rakesh S. Integrated nutrient management strategies for rainfed agro-ecosystems of India. Indian J Fert. 2020;16(4):344–61.
  77. 77. Ata-Ul-Karim ST, Liu X, Lu Z, Yuan Z, Zhu Y, Cao W. In-season estimation of rice grain yield using critical nitrogen dilution curve. Field Crops Res. 2016;195:1–8. https://doi.org/10.1016/j.fcr.2016.04.027
  78. 78. Saud S, Fahad S, Yajun C, Ihsan MZ, Hammad HM, Nasim W, et al. Effects of nitrogen supply on water stress and recovery mechanisms in Kentucky bluegrass plants. Front Plant Sci. 2017;8:983. https://doi.org/10.3389/fpls.2017.00983
  79. 79. Tran TT, Kano-Nakata M, Takeda M, Menge D, Mitsuya S, Inukai Y, et al. Nitrogen application enhanced the expression of developmental plasticity of root systems triggered by mild drought stress in rice. Plant Soil. 2014;378:139–52. https://doi.org/10.1007/s11104-013-2013-5
  80. 80. Tarvainen L, Näsholm T. Can adjustments in foliar nitrogen-use efficiency reduce drought stress impacts on boreal trees? Tree Physiol. 2017;37:415–7. https://doi.org/10.1093/treephys/tpx003
  81. 81. Tariq A, Pan K, Olatunji OA, Graciano C, Li Z, Sun F, et al. Phosphorous application improves drought tolerance of Phoebe hennan. Front Plant Sci. 2017;8:1561. https://doi.org/10.3389/fpls.2017.01561
  82. 82. Bechtaoui N, Rabiu MK, Raklami A, Oufdou K, Hafidi M, Jemo M. Phosphate-dependent regulation of growth and stress management in plants. Front Plant Sci. 2021;12:679916. https://doi.org/10.3389/fpls.2021.679916
  83. 83. Tariq A, Pan K, Olatunji OA, Graciano C, Li Z, Sun F, et al. Phosphorus fertilisation alleviates drought effects on Alnus cremastogyne by regulating its antioxidant and osmotic potential. Sci Rep. 2018;8:5644. https://doi.org/10.1038/s41598-018-24038-2
  84. 84. Begum N, Ahanger MA, Zhang L. AMF inoculation and phosphorus supplementation alleviate drought-induced growth and photosynthetic decline in Nicotiana tabacum by up-regulating antioxidant metabolism and osmolyte accumulation. Environ Exp Bot. 2020;176:104088. https://doi.org/10.1016/j.envexpbot.2020.104088
  85. 85. Dey G, Banerjee P, Sharma RK, Maity JP, Etesami H, Shaw AK, et al. Management of phosphorus in salinity-stressed agriculture for sustainable crop production by salt-tolerant phosphate-solubilising bacteria: a review. Agron. 2021;11:1552. https://doi.org/10.3390/agronomy11081552
  86. 86. Wang Y, Zhang H, Huang X. Effect of potassium supply on plant potassium distribution and growth and leaf photosynthetic capacity of Pyrus pyrifolia. J Nanjing Agric Univ. 2017;40:60–7. https://doi.org/10.3389/fpls.2020.00904
  87. 87. Banerjee P, Ghosh A, Kumari VV, Nath R. Effect of canopy temperature on physiological processes of grass pea as influenced by seed priming and foliar fertilisation. J Agrometeorol. 2021;23:340–3. https://doi.org/10.54386/jam.v23i3.39
  88. 88. Rahman A, Mostofa MG, Alam MM, Nahar K, Hasanuzzaman M, Fujita M. Calcium mitigates arsenic toxicity in rice seedlings by reducing arsenic uptake and modulating the antioxidant defence and glyoxalase systems and stress markers. Biomed Res Int. 2015;2015:340812. https://doi.org/10.1155/2015/340812
  89. 89. Duman F. Abiotic stress responses in plants. In: Uptake of mineral elements during abiotic stress. New York, NY: Springer; 2012. p. 267–81. https://doi.org/10.1007/978-1-4614-0634-1_15
  90. 90. Mei J, Wang W, Peng S, Nie L. Seed pelleting with calcium peroxide improves crop establishment of direct-seeded rice under waterlogging conditions. Sci Rep. 2017;7:4878. https://doi.org/10.1038/s41598-017-04966-1
  91. 91. Cao MJ, Wang Z, Zhao Q, Mao JL, Speiser A, Wirtz M, et al. Sulfate availability affects ABA levels and germination response to ABA and salt stress in Arabidopsis thaliana. Plant J. 2014;77:604–15. https://doi.org/10.1111/tpj.12407
  92. 92. Liu H, Wang J, Liu J, Liu T, Xue S. Hydrogen sulfide (H₂S) signalling in plant development and stress responses. Abiotech. 2021;2:32–63. https://doi.org/10.1007/s42994-021-00035-4
  93. 93. Shahid M, Nayak AK, Tripathi R, Katara JL, Bihari P, Lal B, et al. Boron application improves yield of rice cultivars under high temperature stress during vegetative and reproductive stages. Int J Biometeorol. 2018;62:1375–87. https://doi.org/10.1007/s00484-018-1537-1
  94. 94. Venugopalan VK, Roy A, Vijayan R, Banerjee P, Verma VC, Nalia A, et al. Drought and heat stress in cool-season food legumes in sub-tropical regions: consequences, adaptation and mitigation strategies. Plants. 2021;10:1038. https://doi.org/10.3390/plants10061038
  95. 95. Bashir K, Rasheed S, Kobayashi T, Seki M, Nishizawa NK. Regulating subcellular metal homeostasis: the key to crop improvement. Front Plant Sci. 2016;7:1192. https://doi.org/10.3389/fpls.2016.01192
  96. 96. Nadeem F, Farooq M. Application of micronutrients in rice–wheat cropping system of South Asia. Rice Sci. 2019;26:356–71. https://doi.org/10.1016/j.rsci.2019.02.002
  97. 97. Daneshbakhsh B, Khoshgoftarmanesh AH, Shariatmadari H, Cakmak I. Effect of zinc nutrition on salinity-induced oxidative damages in wheat genotypes differing in zinc deficiency tolerance. Acta Physiol Plant. 2013;35:881–9. https://doi.org/10.1007/s11738-012-1131-7
  98. 98. Balk J, Pilon M. Ancient and essential: the assembly of iron–sulfur clusters in plants. Trends Plant Sci. 2011;16:218–26. https://doi.org/10.1016/j.tplants.2010.12.006
  99. 99. Hasanpour H, Maali-Amir R, Zeinali H. Effect of TiO₂ nanoparticles on metabolic limitations to photosynthesis under cold in chickpea. Russ J Plant Physiol. 2015;62:779–87. https://doi.org/10.1134/S1021443715060096
  100. 100. Zhang X, Goatley M, Conner J, Wilkins M, Teshler I, Liu J, et al. Copper chlorophyllin impacts on growth and drought stress tolerance of tomato plants. HortScience. 2019;54:2195–201. https://doi.org/10.21273/HORTSCI14434-19
  101. 101. Hejazi MM, Shariatmadari H, Khoshgoftarmanesh AH, Dehghani F. Copper effects on growth, lipid peroxidation and total phenolic content of rosemary leaves under salinity stress. J Agric Sci Technol. 2019;21:2195–201.
  102. 102. Iqbal S, Waheed Z, Naseem A. Nanotechnology and abiotic stresses. In: Javad S, editor. Nanoagronomy. Cham, Switzerland: Springer; 2020. p. 37–52. https://doi.org/10.1007/978-3-030-41275-3_3
  103. 103. Pranjit PK, Hazarika M, Sarma D, Saikia P, Kumar NP, Rajbongshi R, et al. Effect of foliar application of potassium on yield, drought tolerance and rainwater use efficiency of toria under rainfed upland situation of Assam. Indian J Dryland Agric Res Dev. 2015;30:55–9. https://doi.org/10.5958/2231-6701.2015.00008.1
  104. 104. Abid M, Tian Z, Ata-Ul-Karim ST, Cui Y, Liu Y, Zahoor R, et al. Nitrogen nutrition improves the potential of wheat (Triticum aestivum L.) to alleviate the effects of drought stress during vegetative growth periods. Front Plant Sci. 2016;7:981. https://doi.org/10.3389/fpls.2016.00981
  105. 105. Zhang YY, Wang LL, Liu YL, Zhang Q, Wei QP, Zhang WH. Nitric oxide enhances salt tolerance in maize seedlings through increasing activities of proton-pump and Na+/H+ antiport in the tonoplast. Planta. 2006;224:545–55. https://doi.org/10.1007/s00425-006-0242-z
  106. 106. Rostamza M, Chaichi MR, Jahansooz MR, Rahimian Mashhadi H, Sharifi HR. Effects of water stress and nitrogen fertiliser on multi-cut pearl millet forage yield, nitrogen and water use efficiency. Commun Soil Sci Plant Anal. 2011;42:2427–40. https://doi.org/10.1080/00103624.2011.609252
  107. 107. Zain NAM, Ismail MR, Puteh A, Mahmood M, Islam MR. Drought tolerance and ion accumulation of rice following application of additional potassium fertiliser. Commun Soil Sci Plant Anal. 2014;45:2502–14. https://doi.org/10.1080/00103624.2014.932374
  108. 108. Ahanger MA, Agarwal R. Potassium up-regulates antioxidant metabolism and alleviates growth inhibition under water and osmotic stress in wheat (Triticum aestivum L.). Protoplasma. 2017;254:1471–86. https://doi.org/10.1007/s00709-016-1037-0
  109. 109. Ahanger MA, Agarwal R, Tomar NS, Shrivastava M. Potassium induces positive changes in nitrogen metabolism and antioxidant system of oat (Avena sativa L. cultivar Kent). J Plant Interact. 2015;10:211–23. https://doi.org/10.1080/17429145.2015.1056260
  110. 110. Barranco I, Tvarijonaviciute A, Perez-Patiño C, Vicente-Carrillo A, Parrilla I, Ceron JJ, et al. Effect of potassium fertiliser on the growth, physiological parameters and water status of Brassica juncea cultivars under different irrigation regimes. PLoS ONE. 2021;16:e0257023. https://doi.org/10.1371/journal.pone.0257023
  111. 111. Zahoor R, Dong H, Abid M, Zhao W, Wang Y, Zhou Z. Potassium fertiliser improves drought stress alleviation potential in cotton by enhancing photosynthesis and carbohydrate metabolism. Environ Exp Bot. 2017;137:73–83. https://doi.org/10.1016/j.envexpbot.2017.02.002
  112. 112. Roy PR, Tahjib-Ul-Arif M, Polash MAS, Hossen MZ, Hossain MA. Physiological mechanisms of exogenous calcium on alleviating salinity-induced stress in rice (Oryza sativa L.). Physiol Mol Biol Plants. 2019;25:611–24. https://doi.org/10.1007/s12298-019-00654-8
  113. 113. Naeem M, Naeem MS, Ahmad R, Ihsan MZ, Ashraf MY, Hussain Y, et al. Foliar calcium spray confers drought stress tolerance in maize via modulation of plant growth, water relations, proline content and hydrogen peroxide activity. Arch Agron Soil Sci. 2018;64:116–31. https://doi.org/10.1080/03650340.2017.1327713
  114. 114. Guo TR, Chen Y, Zhang YH, Jin YF. Alleviation of Al toxicity in barley by addition of calcium. Agric Sci China. 2006;5:828–33. https://doi.org/10.1016/S1671-2927(06)60131-4
  115. 115. Hosseini SA, Réthoré E, Pluchon S, Ali N, Billiot B, Yvin JC. Calcium application enhances drought stress tolerance in sugar beet and promotes plant biomass and beetroot sucrose concentration. Int J Mol Sci. 2019;20:3777. https://doi.org/10.3390/ijms20153777
  116. 116. Tan W, Meng QW, Brestic M, Olsovska K, Yang X. Photosynthesis is improved by exogenous calcium in heat-stressed tobacco plants. J Plant Physiol. 2011;168:2063–71. https://doi.org/10.1016/j.jplph.2011.06.009
  117. 117. Ding Y, Xu G. Low magnesium with high potassium supply changes sugar partitioning and root growth pattern prior to visible magnesium deficiency in leaves of rice (Oryza sativa L.). Am J Plant Sci. 2011;2:601–8. https://doi.org/10.4236/ajps.2011.24071
  118. 118. Mengutay M, Ceylan Y, Kutman UB, Cakmak I. Adequate magnesium nutrition mitigates adverse effects of heat stress on maize and wheat. Plant Soil. 2013;368:57–72. https://doi.org/10.1007/s11104-013-1761-6
  119. 119. Thalooth AT, Tawfik Mohamed HM. A comparative study on the effect of foliar application of zinc, potassium and magnesium on growth, yield and some chemical constituents of mungbean plants grown under water stress conditions. World J Agric Sci. 2006;2:37–46.
  120. 120. Mahala SC, Singh H, Jat KL, Bajya DR, Khatik CL, Verma KC, et al. Mitigation of drought stress by foliar application of salicylic acid and potassium chloride in cluster bean (Cyamopsis tetragonoloba L.). Agric Sci Dig. 2025. https://doi.org/10.18805/ag.D-6141
  121. 121. El-Okkiah SAF, El-Afry MM, Shehab Eldeen SA, El-Tahan AM, Ibrahim OM, Negm MM, et al. Foliar spray of silica improved water stress tolerance in rice (Oryza sativa L.) cultivars. Front Plant Sci. 2022;13:935090. https://doi.org/10.3389/fpls.2022.935090
  122. 122. Raza MAS, Saleem MF, Shah GM, Jamil M, Khan IH. Potassium applied under drought improves physiological and nutrient uptake performances of wheat (Triticum aestivum L.). J Soil Sci Plant Nutr. 2013;13:175–85.
  123. 123. Farzane A, Nemati H, Shoor M, Ansari H. Foliar application of potassium on antioxidant enzyme activities of tomato plants under drought stress. Adv Hortic Sci. 2020;35:3–9. https://doi.org/10.36253/ahsc-8468
  124. 124. Dixit G, Singh AP, Kumar A, Dwivedi S, Deeba F, Smita K, et al. Sulfur alleviates arsenic toxicity by reducing its accumulation and modulating proteome, amino acids and thiol metabolism in rice leaves. Sci Rep. 2015;5:16205. https://doi.org/10.1038/srep16205
  125. 125. Cao ZZ, Qin ML, Lin XY, Zhu ZW, Chen MX. Sulfur supply reduces cadmium uptake and translocation in rice grains (Oryza sativa L.) by enhancing iron plaque formation, cadmium chelation and vacuolar sequestration. Environ Pollut. 2018;238:76–84. https://doi.org/10.1016/j.envpol.2018.02.083
  126. 126. Chen J, Wang WH, Wu FH, He EM, Liu X, Shangguan ZP, et al. Hydrogen sulfide enhances salt tolerance through nitric oxide-mediated maintenance of ion homeostasis in barley seedling roots. Sci Rep. 2015;5:12516. https://doi.org/10.1038/srep12516
  127. 127. Dawood M, Cao F, Jahangir MM, Zhang G, Wu F. Alleviation of aluminium toxicity by hydrogen sulfide is related to elevated ATPase and suppressed aluminium uptake and oxidative stress in barley. J Hazard Mater. 2012;209:121–8. https://doi.org/10.1016/j.jhazmat.2011.12.076
  128. 128. Ahmad W, Waraich EA, Haider A, Mahmood N, Ramzan T, Alamri S, et al. Silicon-mediated improvement in drought and salinity stress tolerance of black gram (Vigna mungo L.) by modulating growth, physiological, biochemical and root attributes. ACS Omega. 2024;9(35):37231–42. https://doi.org/10.1021/acsomega.4c04727
  129. 129. Bukhari MA, Ahmad Z, Ashraf MY, Afzal M. Silicon mitigates drought stress in wheat (Triticum aestivum L.) through improving photosynthetic pigments, biochemical and yield characters. Silicon. 2021;13:4371–80. https://doi.org/10.1007/s12633-020-00797-4
  130. 130. Bansal K, Hooda V, Verma N, Kharewal T, Tehri N, Dhull V, et al. Stress alleviation and crop improvement using silicon nanoparticles in agriculture: a review. Silicon. 2022;14:10173–10186. https://doi.org/10.1007/s12633-022-01755-y
  131. 131. Kumar A, Suri VK, Choudhary AK. Influence of inorganic phosphorus, VAM fungi and irrigation regimes on crop productivity and phosphorus transformations in okra (Abelmoschus esculentus L.)–pea (Pisum sativum L.) cropping system in an acid alfisol. Commun Soil Sci Plant Anal. 2014;45:953–67. https://doi.org/10.1080/00103624.2013.874025
  132. 132. Suri VK, Choudhary AK. Effect of VAM fungi and phosphorus application through STCR precision model on crop productivity, nutrient dynamics and soil fertility in soybean–wheat–soybean crop sequence in an acid alfisol. Commun Soil Sci Plant Anal. 2013;44:2032–41. https://doi.org/10.1080/00103624.2013.783921
  133. 133. Wang M, Zheng Q, Shen Q, Guo S. The critical role of potassium in plant stress response. Int J Mol Sci. 2013;14:7370–90. https://doi.org/10.3390/ijms14047370
  134. 134. Farooq M, Basra SMA, Rehman H, Saleem BA. Seed priming enhances the performance of late-sown wheat (Triticum aestivum L.) by improving chilling tolerance. J Agron Crop Sci. 2008;194:55–60. https://doi.org/10.1111/j.1439-037X.2007.00287.x
  135. 135. Oosterhuis DM, Loka DA, Raper TB. Potassium and stress alleviation: physiological functions and management of cotton. J Plant Nutr Soil Sci. 2013;176:331–43. https://doi.org/10.1002/jpln.201200414
  136. 136. Dwivedi SK, Kumar S, Bhakta N, Singh SK, Rao KK, Mishra JS, et al. Improvement of submergence tolerance in rice through efficient application of potassium under submergence-prone rainfed ecology of the Indo-Gangetic plain. Plant Biol. 2017;44:907–16. https://doi.org/10.1071/FP17054
  137. 137. Naciri R, Lahrir M, Benadis C, Chtouki M, Oukarroum A. Interactive effect of potassium and cadmium on growth, root morphology and chlorophyll a fluorescence in tomato plant. Sci Rep. 2021;11:1–10. https://doi.org/10.1038/s41598-021-83967-5
  138. 138. Treder W, Cieslinski G. Effect of silicon application on cadmium uptake and distribution in strawberry plants grown on contaminated soils. J Plant Nutr. 2005;28:917–29. https://doi.org/10.1081/PLN-200058877
  139. 139. Karunarathne WMA, Subasinghe S, Kumarasinghe HKMS, Adikaram KKLB, Piyaratne MKDK. Growth and yield of Capsicum annuum (bell pepper) as affected by application rates and splits of Albert’s fertiliser under protected cultivation in the low country wet zone of Sri Lanka. J Agro-Technol Rural Sci. 2024;4:14–22. https://doi.org/10.4038/atrsj.v4i2.61
  140. 140. Siddiqui MH, Whaibi AL, Sakran AM, Basalah MO, Ali HM. Effect of calcium and potassium on the antioxidant system of Vicia faba L. under cadmium stress. Int J Mol Sci. 2012;13:6604–19. https://doi.org/10.3390/ijms13066604
  141. 141. Song ZZ, Duan CL, Guo SL, Yang Y, Feng YF, Ma RJ, et al. Potassium contributes to zinc stress tolerance in peach (Prunus persica) seedlings by enhancing photosynthesis and the antioxidant defence system. Genet Mol Res. 2015;14:8338–51. https://doi.org/10.4238/2015.July.27.22
  142. 142. Zaheer MM, Yasin NA, Ahmad SR, Khan WU, Ahmad A, Ali A, et al. Amelioration of cadmium stress in gladiolus (Gladiolus grandiflora L.) by application of potassium and silicon. J Plant Nutr. 2017;40:461–76. https://doi.org/10.1080/01904167.2017.1385808
  143. 143. Do EA, Gries CM. Beyond homeostasis: potassium and pathogenesis during bacterial infections. Infect Immun. 2021.
  144. 144. Pandey R. Controlling tobacco diseases: an overview of black shank and fusarium wilt. Int J Appl Sci Biotechnol. 2023;11:1–7. https://doi.org/10.3126/ijasbt.v11i1.52440
  145. 145. Bakhat FZ, Bibi N, Zia Z, Abbas S, Hammad HM, Fahad S, et al. Silicon mitigates biotic stresses in crop plants: a review. Crop Prot. 2018;104:21–34. https://doi.org/10.1016/j.cropro.2017.10.008
  146. 146. Jeer M, Suman K, Telugu UM, Voleti SR, Padmakumari AP. Rice husk ash and imidazole application enhances silicon availability to rice plants and reduces yellow stem-borer damage. Field Crops Res. 2018;224:60–6. https://doi.org/10.1016/j.fcr.2018.05.002
  147. 147. Rosskopf EN, Di Gioia F, Hong JC, Pisani C, Kokalis-Burelle N. Organic amendments for pathogen and nematode control. Annu Rev Phytopathol. 2020;58:277–311. https://doi.org/10.1146/annurev-phyto-080516-035608
  148. 148. Yatoo AM, Ali MN, Baba ZA, Hassan B. Sustainable management of diseases and pests in crops by vermicompost and vermicompost tea: a review. Agron Sustain Dev. 2021;41:7. https://doi.org/10.1007/s13593-020-00657-w
  149. 149. Kousta A, Papastylianou P, Travlos I, Mavroeidis A, Kakabouki I. Effect of fertilisation and weed management practices on weed diversity and hemp agronomic performance. Agron. 2023;13:1060. https://doi.org/10.3390/agronomy13041060
  150. 150. Stewart CJ, Marble SC, Jackson BE, Pearson BJ, Wilson PC. Effects of three fertilisation methods on weed growth and herbicide performance in soilless nursery substrates. J Environ Hortic. 2018;36:133–9. https://doi.org/10.24266/0738-2898-36.4.133
  151. 151. Prabhu KV, Bhattacharya PM. Influence of potassium on leaf rust severity in wheat. Indian J Agric Sci. 2002;72:163–5.
  152. 152. Datnoff LE, Deren CW, Snyder GH. Silicon fertilisation for disease management of rice in Florida. Crop Prot. 1997;16:525–31. https://doi.org/10.1016/S0261-2194(97)00033-9
  153. 153. Huber DM, Thompson IA. Nitrogen and plant disease. In: Datnoff LE, Elmer WH, Huber DM, editors. Mineral nutrition and plant disease. APS Press; 2007. p. 31–44.
  154. 154. Savvas D, Ntatsi G. Biostimulant role of silicon in horticulture. Sci Hortic. 2015;196:66–8. https://doi.org/10.1016/j.scienta.2015.09.010
  155. 155. Fauteux F, Remus-Borel W, Menzies JG, Bélanger RR. Silicon and plant disease resistance against pathogenic fungi. FEMS Microbiol Lett. 2005;249:1–6. https://doi.org/10.1016/j.femsle.2005.06.034
  156. 156. Lal MK, Tiwari RK, Kumar R, Gautam NK. Effect of potassium and organic manure on growth, yield and incidence of anthracnose in chilli (Capsicum annuum L.). Veg Sci. 2019;46:174–9.

Downloads

Download data is not yet available.